Bupivacaine Hydrochloride Injection, Solution
Product Images NDC 83854-004

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Bupivacaine Hydrochloride (NDC 83854-004). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Anthea Pharma Private Limited, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

"image Description" (Bupi Cart Lab 225mg 30ml)

"image Description" (Bupi Cart Lab 225mg 30ml)
Bupivacaine Hydrochloride Injection, USP 0.75% (225 mg/30 mL or 7.5 mg/mL) in injection solution form. The label states it is preservative-free and intended for epidural and retrobulbar anesthesia, explicitly noting it is not for obstetric or intrathecal anesthesia. The package contains 10 single-dose vials of 30 mL each. Manufactured by Anthea Pharma Private Limited.*
FDA Label Image

"image Description" (Bupi Cart Lab 250mg 50ml)

"image Description" (Bupi Cart Lab 250mg 50ml)
Bupivacaine Hydrochloride Injection, USP 0.5% (5 mg/mL) in a 250 mg/50 mL multiple-dose vial. The label indicates it is for nerve block use and explicitly states it is not for caudal, epidural, or intrathecal anesthesia. Manufactured by Anthea Pharma Private Limited, Hyderabad, India. Storage and dosage information is included, along with a barcode and regulatory details.*
FDA Label Image

"image Description" (Bupi Cart Lab 25mg 10ml)

"image Description" (Bupi Cart Lab 25mg 10ml)
Packaging label for Bupivacaine Hydrochloride Injection, USP 0.25% (25 mg/10 mL) solution for injection by Anthea Pharma Private Limited. The label states it is preservative-free and intended for infiltration, nerve block, caudal, and epidural anesthesia, not for intrathecal anesthesia. The package contains 10 single-dose 10 mL vials.*
FDA Label Image

"image Description" (Bupi Cont Lab 225mg 30ml)

"image Description" (Bupi Cont Lab 225mg 30ml)
Label for Bupivacaine Hydrochloride Injection, USP 0.75% (7.5 mg/mL) in a 30 mL single-dose vial, containing 225 mg per vial. The preservative-free solution is for epidural and retrobulbar anesthesia, manufactured by Anthea Pharma Private Limited in Hyderabad, India. Storage instructions and lot/expiration placeholders are also shown.*
FDA Label Image

"image Description" (Bupi Cont Lab 250mg 50ml)

"image Description" (Bupi Cont Lab 250mg 50ml)
Bupivacaine Hydrochloride Injection, USP 5 mg/mL (0.5%) solution in a 50 mL multiple-dose vial. The label specifies use for nerve block and states it is not for caudal, epidural, or intrathecal anesthesia. Manufactured by Anthea Pharma Private Limited, Hyderabad, India, with storage instructions and lot/expiration date fields.*
FDA Label Image

"image Description" (Bupi Cont Lab 25mg 10ml)

"image Description" (Bupi Cont Lab 25mg 10ml)
Label for Bupivacaine Hydrochloride Injection, USP 0.25% (25 mg/10 mL or 2.5 mg/mL) in a 10 mL single-dose vial. The label states it is preservative-free and intended for infiltration, nerve block, caudal, and epidural anesthesia, but not for intrathecal anesthesia. Manufactured by Anthea Pharma Private Limited, Hyderabad, India. Includes storage and usage instructions with lot and expiration date placeholders.*
FDA Label Image

"image Description" (Spl Structure Bupivacaine)

"image Description" (Spl Structure Bupivacaine)
Chemical structure of Bupivacaine Hydrochloride showing its molecular composition with labeled atoms and bonds, including the hydrochloride and water components.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.